Canonical Allele Identifier: CA499890722

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143299422
• MyVariant Identifiers: chr17:g.37884066G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727813G>C , CM000679.2:g.39727813G>C	GRCh38
NC_000017.10:g.37884066G>C , CM000679.1:g.37884066G>C	GRCh37
NC_000017.9:g.35137592G>C	NCBI36
NG_007503.1:g.44674G>C , LRG_724:g.44674G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3537G>C MANE Select	ENSP00000269571.4:p.Gly1179=
ENST00000269571.9:c.3537G>C	ENSP00000269571.4:p.Gly1179=
ENST00000406381.6:c.3447G>C	ENSP00000385185.2:p.Gly1149=
ENST00000445658.6:c.2709G>C	ENSP00000404047.2:p.Gly903=
ENST00000541774.5:c.3492G>C	ENSP00000446466.1:p.Gly1164=
ENST00000578373.5:c.*3327G>C	ENSP00000463427.1:n.*3327G>C
ENST00000584450.5:c.*116G>C	ENSP00000463714.1:n.*116G>C
ENST00000584601.5:c.3447G>C	ENSP00000462438.1:p.Gly1149=
NM_001005862.2:c.3447G>C , LRG_724t1:c.3447G>C	NP_001005862.1:p.Gly1149=
NM_001289936.1:c.3492G>C , LRG_724t4:c.3492G>C	NP_001276865.1:p.Gly1164=
NM_001289937.1:c.*116G>C	NP_001276866.1:n.*116G>C
NM_004448.3:c.3537G>C , LRG_724t2:c.3537G>C	NP_004439.2:p.Gly1179=
NR_110535.1:n.3861G>C
XM_024450641.1:c.3675G>C	XP_024306409.1:p.Gly1225=
XM_024450642.1:c.3630G>C	XP_024306410.1:p.Gly1210=
XM_024450643.1:c.3585G>C	XP_024306411.1:p.Gly1195=
NM_001005862.3:c.3447G>C	NP_001005862.1:p.Gly1149=
NM_001289936.2:c.3492G>C	NP_001276865.1:p.Gly1164=
NM_001289937.2:c.*116G>C	NP_001276866.1:n.*116G>C
NM_001382782.1:c.3447G>C	NP_001369711.1:p.Gly1149=
NM_001382783.1:c.3447G>C	NP_001369712.1:p.Gly1149=
NM_001382784.1:c.3654G>C	NP_001369713.1:p.Gly1218=
NM_001382785.1:c.3639G>C	NP_001369714.1:p.Gly1213=
NM_001382786.1:c.3618G>C	NP_001369715.1:p.Gly1206=
NM_001382787.1:c.3612G>C	NP_001369716.1:p.Gly1204=
NM_001382788.1:c.3567G>C	NP_001369717.1:p.Gly1189=
NM_001382789.1:c.3558G>C	NP_001369718.1:p.Gly1186=
NM_001382790.1:c.3534G>C	NP_001369719.1:p.Gly1178=
NM_001382791.1:c.3528G>C	NP_001369720.1:p.Gly1176=
NM_001382792.1:c.3501G>C	NP_001369721.1:p.Gly1167=
NM_001382793.1:c.3495G>C	NP_001369722.1:p.Gly1165=
NM_001382794.1:c.3495G>C	NP_001369723.1:p.Gly1165=
NM_001382795.1:c.3489G>C	NP_001369724.1:p.Gly1163=
NM_001382796.1:c.3450G>C	NP_001369725.1:p.Gly1150=
NM_001382797.1:c.3438G>C	NP_001369726.1:p.Gly1146=
NM_001382798.1:c.3381G>C	NP_001369727.1:p.Gly1127=
NM_001382799.1:c.3357G>C	NP_001369728.1:p.Gly1119=
NM_001382800.1:c.3351G>C	NP_001369729.1:p.Gly1117=
NM_001382801.1:c.3333G>C	NP_001369730.1:p.Gly1111=
NM_001382802.1:c.3279G>C	NP_001369731.1:p.Gly1093=
NM_001382803.1:c.*116G>C	NP_001369732.1:n.*116G>C
NM_001382804.1:c.2709G>C	NP_001369733.1:p.Gly903=
NM_001382805.1:c.2586G>C	NP_001369734.1:p.Gly862=
NM_001382806.1:c.2499G>C	NP_001369735.1:p.Gly833=
NM_004448.4:c.3537G>C MANE Select	NP_004439.2:p.Gly1179=
NR_110535.2:n.3775G>C